Cancer in Fanconi anemia, 1927-2001

Cancer

Volumn 97, Issue 2, 2003, Pages 425-440

  Alter, Blanche P ^a  

^a NONE

Author keywords

Aplastic anemia; Bone marrow transplant; Cancer; Fanconi anemia; Leukemia; Liver tumor; Malignancy; Myelodysplastic syndrome

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ADOLESCENT; ADULT; APLASTIC ANEMIA; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BONE MARROW TRANSPLANTATION; CANCER; CANCER RISK; CHILD; DIGESTIVE SYSTEM TUMOR; FANCONI ANEMIA; FEMALE; GENETIC MODEL; GYNECOLOGIC CANCER; HEAD AND NECK CANCER; HUMAN; INFANT; LEUKEMIA; LIVER TUMOR; MAJOR CLINICAL STUDY; MALE; MYELODYSPLASTIC SYNDROME; PRIORITY JOURNAL; SOLID TUMOR;

EID: 0037439356     PISSN: 0008543X     EISSN: None     Source Type: Journal    
DOI: 10.1002/cncr.11046     Document Type: Article

References (221)

1. Alter BP. Inherited bone marrow failure syndromes. In: Nathan DG, Orkin S, Ginsburg D, Look T. Hematology of infancy and childhood, 6th ed. Philadelphia: Harcourt Health Sciences. In press.
2. Nichols KE, Malkin D, Garber JE, Fraumeni JF Jr., Li FP. Germ-line p53 mutations predispose to a wide spectrum of early-onset cancers. Cancer Epidemiol Biomarkers Prev. 2001;10:83-87.
3. Friend SH, Horowitz JM, Gerber MR, et al. Deletions of a DNA sequence in retinoblastomas and mesenchymal tumors: organization of the sequence and its encoded protein. Proc Natl Acad Sci USA. 1987;84:9059-9063.
4. Fearon ER. Human cancer syndromes: clues to the origin and nature of cancer. Science. 1997;278:1043-1050.
5. Abeloff MD, Armitage JO, Lichter AS, Niederhuber JE. Clinical oncology, 2nd ed. New York: Churchill Livingstone, 2000.
6. Joenje H, Patel KJ. The emerging genetic and molecular basis of Fanconi anaemia. Nat Rev Genet. 2001;2:446-459.
7. Garcia-Higuera I, Taniguchi T, Ganesan S, et al. Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway. Mol Cell. 2001;7:249-262.
8. Matsson H, Klar J, Draptchinskaia N, et al. Truncating ribosomal protein S19 mutations and variable clinical expression in Diamond-Blackfan anemia. Hum Genet. 1999;105:496-500.
9. Knight SW, Heiss NS, Vulliamy TJ, et al. X-linked dyskeratosis congenita is predominantly caused by missense mutations in the DKC1 gene. Am J Hum Genet. 1999;65:50-58.
10. Vulliamy T, Marrone A, Goldman F, et al. The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita. Nature. 2001;413:432-435.
11. Dale DC, Person RE, Bolyard AA, et al. Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia. Blood. 2000;96:2317-2322.
12. Ballmaier M, Germeshausen M, Schulze H, et al. C-mpl mutations are the cause of congenital amegakaryocytic thrombocytopenia. Blood. 2001;97:139-146.
13. Goobie S, Popovic M, Morrison J, et al. Shwachman-Diamond syndrome with exocrine pancreatic dysfunction and bone marrow failure maps to the centromeric region of chromosome 7. Am J Hum Genet. 2001;68:1048-1054.
14. Alter BP. Fanconi's anemia and malignancies. Am J Hematol. 1996;53:99-110.
15. StataCorp. Stata statistical software: release 7.0. College Station, TX: Stata, 2001.
16. Kaplan EL, Meier P. Nonparametric estimation from incomplete observations. J Am Stat Assoc. 1958;53:457-481.
17. Alter BP, Caruso JP, Drachtman RA, Uchida T, Elghetany MT. Fanconi's anemia: myelodysplasia as a predictor of outcome. Cancer Genet Cytogenet. 2000;117:125-131.
18. Pizzo PA, Poplack DG. Principles and practice of pediatric oncology, 3rd ed. Philadelphia: Lippincott-Raven, 1997.
19. Ahmed OA, Al-Rimawi HS, Al-Rashid AA, et al. Fanconi's anemia with acute lymphoblastic leukaemia in a Bedouin girl. Am Soc Hum Genet. 1989;45(Suppl):A14.
20. Wada E, Murata M, Watanabe S. Acute lymphoblastic leukemia following treatment by human growth hormone in a boy with possible preanemic Fanconi's anemia. Jpn J Clin Oncol. 1989;19:36-39.
21. Yetgin S, Tuncer M, Guler E, Duru F, Kasifoglu ME. Acute lymphoblastic leukemia in Fanconi's anemia. Am J Hematol. 1994;45:94.
22. Tezcan I, Tuncer M, Uckan D, et al. Allogeneic bone marrow transplantation in Fanconi anemia from Turkey: a report of four cases. Pediatr Transpl. 1998;2:236-239.
23. Sugita K, Taki T, Hayashi Y, et al. MLL-CBP fusion transcript in a therapy-related acute myeloid leukemia with the t(11;16)(q23;p13) which developed in an acute lymphoblastic leukemia patient with Fanconi anemia. Genes Chromosomes Cancer. 2000;27:264-269.
24. Janik-Moszant A, Bubala H, Stojewska M, Sonta-Jakimczyk D. Acute lymphoblastic leukaemia in children with Fanconi anaemia. Wiad Lek. 1998;51:285-288.
25. Skikne BS, Lynch SR, Bezwoda WR, et al. Fanconi's anaemia, with special reference to erythrokinetic features. S Afr Med J. 1978;53:43-50.
26. Meisner LF, Taher A, Shahidi NT. Chromosome changes and leukemic transformation in Fanconi's anemia. In: Hibino S, Takaku F, Shahidi NT. Aplastic anemia. Tokyo: University of Tokyo Press, 1976:253-271.
27. Eldar M, Shoenfeld Y, Zaizov R, et al. Pulmonary alveolar proteinosis associated with Fanconi's anemia. Respiration. 1979;38:177-179.
28. Perona G, Cetto GL, Bernardi F, Todeschini G, D'Andrea F. Fanconi's anaemia in adults: study of three families. Haematologica. 1977;62:615-628.
29. Schaison G, Leverger G, Yildiz C, Berger R, Bemheim A, Gluckman E. L'anemie de Fanconi. Frequence de l'evolution vers la leucemie. [Fanconi's anemia. Incidence of its development into leukemia] Presse Med. 1983;12:1269-1274.
30. Altay C, Alikasifoglu M, Kara A, Tuncbilek E, Ozbek N, Schroeder-Kurth TM. Analysis of 65 Turkish patients with congenital aplastic anemia: (Fanconi anemia and non-Fanconi anemia): Hacettepe experience. Clin Genet. 1997;51:296-302.
31. Verbeek W, Haase D, Schoch C, Hiddemann W, Wormann B. Induction of a hematological and cytogenetic remission in a patient with a myelodysplastic syndrome secondary to Fanconi's anemia employing the S-HAM regimen. Ann Hematol. 1997;74:275-277.
32. Zawartka M, Restorff-Libiszowska H, Kowalski R, Litwiniszyn-Krzewicka K, Schejbal J. Bialaczka szpikowa w prezebiegu anemii Fanconiego (AF) [Myeloid leukemia during Fanconi's anemia]. Wiad Lek. 1976;29:145-151.
33. Perrimond H, Juhan-Vague I, Thevenieau D, Bayle J, Muratore R, Orsini A. Evolution medullaire et hepatique apres androgenotherapie prolongee d'une anemie de Fanconi [Bone marrow and hepatic evolution after prolonged androgen therapy in Fanconi anemia]. Nouv Rev Fr Hematol. 1977;18:228.
34. Kapelushnik J, Or R, Slavin S, Nagler A. A fludarabine-based protocol for bone marrow transplantation in Fanconi's anemia. Bone Marrow Transplant. 1997;20:1109-1110.
35. Van Gils JE, Mandel C, Van Weel-Sipman MH, De Koning J, Van'T Veer-Korthof ET. Acute leukemie bij Fanconi anemie [Acute leukemia of Fanconi's anemia]. Tijdschr Kindergeneeskd. 1987;55:68-72.
36. El Mauhoub M, Sudarshan G, Banerjee G, Aggarwal VP, Shembish N. Fanconi's anemia with associated acute nonlymphocytic leukemia. Indian Pediatr. 1988;25:1124-1127.
37. Submoke S, Kessacorn W. Fanconi's syndrome: presentation of a case of acute myeloblastic leukemia. J Med Assoc Thai. 1985;68:480-484.
38. Barton JC, Parmley RT, Carroll AJ, Huang ST, Goodnough LT, Findley HW Jr. Preleukemia in Fanconi's anemia: hematopoietic cell multinuclearity, membrane duplication, and dysgranulogenesis. J Submicrosc Cytol. 1987;19:355-364.
39. Tanzer J, Frocrain C, Desmarest MC. Anomalies du chromosome 1 dans 3 cas de leucemie compliquant une aplasie de Fanconi (FA) [Anomalies of chromosome 1 in 3 cases of leukemia complicating Fanconi anemia (FA)]. Nouv Rev Fr Hematol. 1980;22:93.
40. Nowell P, Bergman G, Besa E, Wilmoth D, Emanuel B. Progressive preleukemia with a chromosomally abnormal clone in a kindred with the Estren-Dameshek variant of Fanconi's anemia. Blood. 1984;64:1135-1138.
41. Woods WG, Nesbit ME, Buckley J, et al. Correlation of chromosome abnormalities with patient characteristics, histologic subtype, and induction success in children with acute nonlymphocytic leukemia. J Clin Oncol. 1985;3:3-11.
42. Maarek O, Jonveaux P, Le Coniat M, Berger R. Faconi anemia and bone marrow clonal chromosome abnormalities. Leukemia. 1996;10:1700-1704.
43. Obeid A, Hill FGH, Harnden D, Mann JR, Wood BSB. Fanconi anemia: oxymetholone hepatic tumors and chromosome aberrations associated with leukemic transition. Cancer. 1980;46:1401-1404.
44. Auerbach AD, Weiner M, Warburton D, Yeboa K, Lu L, Broxmeyer HE. Acute myeloid leukemia as the first hematologic manifestation of Fanconi anemia. Am J Hematol. 1982;12:289-300.
45. Berger R, Bussel A, Schenmetzler C. Somatic segregation and Fanconi anemia. Clin Genet. 1977;11:409-415.
46. Berger R, Le Coniat M. Cytogenetic studies in Fanconi anemia induced chromosomal breakage and cytogenetics. In: Schroeder-Kurth TM, Auerbach AD, Obe G. Fanconi anemia. Clinical, cytogenetic and experimental aspects. Berlin: Springer-Verlag, 1989:93-99.
47. Berger R, le Coniat M, Schaison G. Chromosome abnormalities in bone marrow of Fanconi anemia patients. Cancer Genet Cytogenet. 1993;65:47-50.
48. Alter BP, Scalise A, McCombs J, Najfeld V. Clonal chromosomal abnormalities in Fanconi's anemia: what do they really mean? Br J Haematol. 1993;85:627-630.
49. Davies SM, Khan S, Wagner JE, et al. Unrelated donor bone marrow transplantation for Fanconi anemia. Bone Marrow Transplant. 1996;17:43-47.
50. Tamary H, Bar-Yam R, Shalmon L, et al. Fanconi anaemia group A (FANCA) mutations in Israeli non-Ashkenazi Jewish patients. Br J Haematol. 2000;111:338-343.
51. Futaki M, Yamashita T, Yagasaki H, et al. The IVS4 +4 A to T mutation of the Fanconi anemia gene FANCC is not associated with a severe phenotype in Japanese patients. Blood. 2000;95:1493-1498.
52. Griffin TC, Friedman DJ, Sanders JM, Bowman WP. Fanconi anemia complicated by acute myelogenous leukemia and malignant brain tumor. Blood. 1992;80:382a.
53. Yoshida Y, Kawabata H, Anzai N. Cell biology and programmed cell death in MDS. Leuk Res. 1994;18:5.
54. Rao AB, Kerketta L, Ghosh K, Mohanty D. A 46, XY, dup(1) (q21q32), add(11) (q23) karyotype in a case of Fanconi anemia. Leuk Res. 2001;25:347-348.
55. Gibbons B, Scott D, Hungerford JL, et al. Retinoblastoma in association with the chromosome breakage syndromes Fanconi's anaemia and Bloom's syndrome: clinical and cytogenetic findings. Clin Genet. 1995;47:311-317.
56. Takizawa J, Kishi K, Moriyama Y, et al. Allogenic bone marrow transplantation for Fanconi's anemia with leukemic transformation from an HLA identical father. Rinsho Ketsueki. 1995;36:615-620.
57. Manglani M, Muralidhar HP, Bhoyar A, Shah R, Lokeshwar MR. Leukemic transformation in Fanconi's anemia. Indian Pediatr. 1999;36:1054-1056.
58. Cowdell RH, Phizackerley PJR, Pyke DA. Constitutional anemia (Fanconi's syndrome) and leukemia in two brothers. Blood. 1955;10:788-801.
59. Sarna G, Tomasulo P, Lotz MJ, Bubinak JF, Shulman NR. Multiple neoplasia in two siblings with a variant form of Fanconi's anemia. Cancer. 1975;36:1029-1033.
60. Consarino C, Magro S, Dattilo A, et al. Acute leukemia in Fanconi's anemia. In: Department of Hematology, University of Rome. Third international symposium on therapy of acute leukemias. Rome: University of Rome Press, 1982:492.
61. O'Gorman Hughes DW. Aplastic anaemia in childhood. III. Constitutional aplastic anaemia and related cytopenias. Med J Austr. 1974;1:519-526.
62. Dosik H, Hsu LY, Todaro GJ, et al. Leukemia in Fanconi's anemia: cytogenetic and tumor virus susceptibility studies. Blood. 1970;36:341-352.
63. Gmyrek D, Witkowski R, Syllm-Rapoport I, Jacobasch G. Chromosomal aberrations and abnormalities of red-cell metabolism in a case of Fanconi's anaemia before and after development of leukaemia. German Med Monthly. 1968;13:105-111.
64. Stein AC, Blanck DM, Bennett AJ, Gold BD, Berger J. Acute myelomonocytic leukemia in a patient with Fanconi's anemia. J Oral Surg. 1981;39:624-627.
65. Gyger M, Bonny Y, Forest L. Childhood monosomy 7 syndrome. Am J Hematol. 1982;13:329-334.
66. Dosik H, Verma RS, Wilson C, Miotti AB. Fanconi's anemia and a familial stable chromosome abnormality in a family with multiple malignancies. Blood. 1977;50:190a.
67. Kunze J. Estren-Dameshek-Anamie mit myelomonocytarer Leukamie (Subtyp der Fanconi-Anamie?) [Estren-Dameshek anemia with myelomonocytic leukemia (subtype of Fanconi anemia?]. In: Spranger J, Tolksdorf M. Klinische Genetik in der Padiatrie. Stuttgart: Thieme, 1980:213-214.
68. Schroeder TM, Tilgen D, Kruger J, Vogel F. Formal genetics of Fanconi's anemia. Hum Genet. 1976;32:257-288.
69. Bloom GE, Warner S, Gerald PS, Diamond LK. Chromosome abnormalities in constitutional aplastic anemia. N Engl J Med. 1966;274:8-14.
70. Bourgeois CA, Hill FGH. Fanconi anemia leading to acute myelomonocytic leukemia, Cytogenetic studies. Cancer. 1977;39:1163-1167.
71. Alimena G, Avvisati G, De Cuia MR, Gallo E, Novelli G, Dallapiccola B. Retrospective diagnosis of a Fanconi's anemia patient by dyepoxybutane (DEB) test results in parents. Haematologica. 1983;68:97-103.
72. Kwee ML, Poll EHA, van de Kamp JJP, de Koning H, Eriksson AW, Joenje H. Unusual response to bifunctional alkylating agents in a case of Fanconi anaemia. Hum Genet. 1983;64:384-387.
73. Roozendaal KJ, Nelis KOAH. Leukaemia in a case of Fanconi's anaemia. Clin Genet. 1981;25:208.
74. McDermott MB, Corbally MT, O'Marcaigh AS. Extracutaneous Sweet syndrome involving the gastrointestinal tract in a patient with Fanconi anemia. J Pediatr Hematol Oncol. 2001;23:59-62.
75. Ortega M, Caballin MR, Ortega JJ, Olive T, Coll MD. Follow-up by cytogenetic and fluorescence in situ hybridization analysis of allogeneic bone marrow transplantation in two children with Fanconi's anaemia in transformation. Br J Haematol. 2000;111:329-333.
76. Ferti A, Panani A, Dervenoulas J, Raptis SA. Cytogenetic findings in a Fanconi anemia patient with AML. Cancer Genet Cytogenet. 1996;90:182-183.
77. Sasaki MS. Fanconi's anemia. A condition possibly associated with a defective DNA repair. In: Hanawalt P, Friedberg EC, Fox CF. DNA repair mechanisms, vol 9. New York: Academic Press, 1978:675-684.
78. Meddeb B, Azzouz MM, Hafsia R, Boussen M. Transformation en leucemie aigue de l'anemia de Fanconi: a propos de 2 cas dans une serie de 21 malades [Transformation of Fanconi's anemia into acute leukemia: apropos of 2 cases in a series of 21 patients]. Tunis Med. 1986;64:755-759.
79. Ahuja HG, Advani SH, Gopal R, Nair CN, Saikia T. Acute nonlymphoblastic leukemia in the first of three siblings affected with Fanconi's syndrome. Am J Pediatr Hematol Oncol. 1986;8:347-349.
80. Gastearena J, Giralt M, Orue MT, Oyarzabal FJ, Perez-Equiza E, Uriz MJ. Fanconi's anemia. Clinical study of six cases. Am J Pediatr Hematol Oncol. 1986;8:173-177.
81. De Vroede M, Feremans W, De Maertelaere-Laurent E, et al. Fanconi's anaemia. Simultaneous onset in 2 siblings and unusual cytological findings. Scand J Haematol. 1982;28:431-440.
82. Stivrins TJ, Davis RB, Sanger W, Fritz J, Purtilo DT. Transformation of Fanconi's anemia to acute nonlymphocytic leukemia associated with emergence of monosomy 7. Blood. 1984;64:173-176.
83. Prindull G, Jentsch E, Hansmann I. Fanconi's anaemia developing erythroleukaemia. Scand J Haematol. 1979;23:59-63.
84. Villegas A, Aboin J, Alvarez-Sala JL, Espinos D. Eritroleucemia en la evolucion de una anemia constitucional de Fanconi [Erythroleukemia in the evolution of a Fanconi's constitutional anemia]. Sangre. 1983;28:225-226.
85. Rotzak R, Kaplinsky N, Chaki R, et al. Giant marker chromosome in Fanconi's anemia transforming into erythroleukemia in an adult. Acta Haematol. 1982;67:214-216.
86. Berger R, Bernheim A, Le Coniat M, Vecchione D, Schaison G. Chromosomal studies of leukemic and preleukemic Fanconi's anemia patients. Examples of acquired 'chromosomal amplification.' Hum Genet. 1980;56:59-62.
87. Zatterale A, Calzone R, Montone E, Pagano G. Il registro Italiano Anemia di Fanconi [The Italian Fanconi Anemia Registry]. Ann 1st Super Sanita. 1999;35:233-235.
88. Dharmasena F, Catchpole M, Erber W, Mason D, Gordon-Smith EC. Megakaryoblastic leukaemia and myelofibrosis complicating Fanconi anaemia. Scand J Haematol. 1986;36:309-313.
89. Athale UH, Ran SR, Kadam PR, et al. Fanconi's anemia: a clinico-hematological and cytogenetic study. Indian Pediatr. 1992;28:1003-1011.
90. Macdougall LG, Greeff MC, Rosendorff J, Bernstein R. Fanconi anemia in Black African children. Am J Med Genet. 1990;36:408-413.
91. Kurtzberg J, Laughlin M, Graham ML, et al. Placental blood as a source of hematopoietic stem cells for transplantation into unrelated recipients. N Engl J Med. 1996;335:157-166.
92. Russo CL, Zwerdling T. Recognition of Fanconi's anemia eight years following treatment for acute nonlymphoblastic leukemia [letter]. Am J Hematol. 1992;40:78-79.
93. Shahid MJ, Khouri FP, Ballas SK. Fanconi's anaemia: report of a patient with significant chromosomal abnormalities in bone marrow cells. J Med Genet. 1972;9:474-478.
94. Gotz M, Pichler E. Zur Panmyelopathie im Kindesalter [Aplasti anemia in childhood]. Klin Paediatr. 1972;148:377-384.
95. Touraine RL, Bertrand Y, Foray P, Gilly J, Philippe N. Hepatic tumours during androgen therapy in Fanconi aneaemia. Eur J Pediatr. 1993;152:691-693.
96. Sanchez MDCE, Cantoni AC, Alvarez BM, et al. Clinical and cytogenetic variability on twelve Fanconi anemia and its relationship with complementation group assignment. Rev Invest Clin. 1999;51:273-283.
97. Hows JM, Chapple M, Marsh JCW, et al. Bone marrow transplantation for Fanconi's anaemia: the Hammersmith experience 1977-89. Bone Marrow Transplant. 1989;4:629-634.
98. Hows JM. Unrelated donor bone marrow transplantation for severe aplastic anaemia and Fanconi's anaemia. Bone Marrow Transplant. 1989;4(Suppl 4):126-128.
99. Schroeder TM. Cytogenetischer Befund und Atiologie bei Fanconi-Anamie. Ein Fall von Fanconi-Anamie ohne Hexokinasedefekt [Cytogenic finding and etiology of Fanconi'e anemia. A case of Fanconi's anemia without hexokinase deficiency]. Humangenetik. 1966;3:76-81.
100. Crossen PE, Mellor JEL, Adams AC, Gunz FW. Chromosome studies in Fanconi's anaemia before and after treatment with oxymetholone. Pathology. 1972;4:27-33.
101. Lisker R, de Gutierrez AC. Cytogenetic studies in Fanconi's anemia. Description of a case with bone marrow clonal evolution. Clin Genet. 1974;5:72-76.
102. Berger R, Bussel A, Schenmetzler C. Anomalies chromosomiques et anemie de Fanconi. Etude de 4 cas [Cytogenetic studies in four cases of Fanconi's anemia]. Nouv Rev Fr Hematol. 1975;15:539-550.
103. Lo Ten Foe JR, Kwee ML, Rooimans MA, et al. Somatic mosaicism in Fanconi anemia: molecular basis and clinical significance. Eur J Hum Genet. 1997;5:137-148.
104. Carbone P, Barbata G, Mirto S, Granata G. Inherited aplastic anemia with abnormal clones in bone marrow and increased endoreduplication in peripheral lymphocytes. Cancer Genet Cytogenet. 1984;13:259-266.
105. Huret JL, Benz E, Guilhot F, Brizard A, Tanzer J. Fluctuation of a clone 46,XX,i(7q) in bone marrow in a Fanconi anaemia. Hum Genet. 1986;74:98-100.
106. Huret JL, Tanzer J, Guilhot F, Frocain-Herchkovitch C, Savage JRK. Karyotype evolution in the bone marrow of a patient with Fanconi anemia: breakpoints in clonal anomalies of this disease. Cytogenet Cell Genet. 1988;48:224-227.
107. Bessho F, Mizutani S, Hayashi Y, Moriwaki K, Yokota S, Inaba T. Chronic myelomonocytic leukemia with chromosomal changes involving 1p36 and hepatocellular carcinoma in a case of Fanconi's anemia. Eur J Haematol. 1989;42:492-495.
108. Baron F, Sybert VP, Andrews RG. Cutaneous and extracutaneous neutrophilic infiltrates (Sweet syndrome) in three patients with Fanconi anemia. J Pediatr. 1989;115:726-729.
109. Standen GR, Hughes IA, Geddes AD, Jones BM, Wardrop CAJ. Myelodysplastic syndrome with trisomy 8 in an adolescent with Fanconi anaemia and selective IgA deficiency. Am J Hematol. 1989;31:280-283.
110. Gluckman E, Devergie A, Bourdeau-Esperou H, et al. Transplantation of umbilical cord blood in Fanconi's anemia. Nouv Rev Fr Hematol. 1991;32:423-425.
111. Gluckman E. European organization for cord blood banking. Blood Cells. 1994;20:601-608.
112. McMullin MF, Mahendra P, Hain R, Barrett AJ. Myelodysplasia as the initial presentation of Fanconi's anaemia in a phenotypically normal child. Clin Lab Haematol. 1991;13:387-389.
113. Scimeca PG, James-Herry AG, Weinblatt ME. Atypical PFAPA syndrome (periodic fever, aphthous stomatitis, pharyngitis, adenitis) in a young girl with Fanconi anemia. J Pediatr. Hematol Oncol. 1996;18:159-161.
114. Kohli-Kumar M, Harris R, Morris C. Bone marrow transplantation in Fanconi anemia with non-sibling donors or following leukemia transformation. Blood. 1992;80:527a.
115. Philpott NJ, Marsh JCW, Kumaran TO, Yardumian A, Lawler M. Successful bone marrow transplant for Fanconi anaemia in transformation. Bone Marrow Transplant. 1994;14:151-153.
116. Mozziconacci MJ, Arnoulet C, Stoppa AM, et al. Anomalies cytogenetiques clonales dans l'anemia de Fanconi [Clonal cytogenetic anomalies in Fanconi anemia]. Nouv Rev Fr Hematol. 1995;37:52-53.
117. Ikushima S, Hibi S, Todo S, et al. Successful allogeneic bone marrow transplantation in a case with myelodysplastic syndrome which developed following Fanconi anemia. Bone Marrow Transplant. 1995;16:621-624.
118. Dokal IS, Roberts IAG. Bone marrow transplantation for Fanconi's anaemia: conditioning with reduced doses of cyclophosphamide without radiation. Br J Haematol. 1996;94:423.
119. Yamamoto M, Hiraumi Y, Ichimura N, et al. Refractory pancreatitis associated with graft-versus-host disease in Fanconi anemia. Am J Hematol. 1996;52:329-330.
120. Hou J-W, Wang T-R. Differentiation of Fanconi anemia from aplastic anemia by chromosomal breakage test. Acta Paediatr Sin. 1997;38:121-126.
121. Thurston VC, Ceperich TM, Vance GH, Heerema NA. Detection of monosomy 7 in bone marrow by fluorescence in situ hybridization. A study of Fanconi anemia patients and review of the literature. Cancer Genet Cytogenet. 1999;109:154-160.
122. Boulad F, Gillio A, Small TN, et al. Stem cell transplantation for the treatment of Fanconi anaemia using a fludarbine-based cytoreductive regimen and T-cell-depleted related HLA-mismatched peripheral blood stem cell grafts. Br J Haematol. 2000;111:1153-1157.
123. Yoshimasu T, Tanaka R, Suenobu S, et al. Prompt and durable hematopoietic reconstitution by unrelated cord blood transplantation in a child with Fanconia anemia. Bone Marrow Transplant. 2001;27:767-769.
124. Nara N, Miyamoto T, Kurisu A, et al. Two siblings with Fanconi's anemia developing squamous cell carcinomas. Rinshou Ketsueki. 1980;21:1944-1950.
125. McDonough ER. Fanconi anemia syndrome. Arch Otolaryngol. 1970;92:284-285.
126. Swift M, Zimmerman D, McDonough ER. Squamous cell carcinomas in Fanconi's anemia. JAMA. 1971;216:325-326.
127. Kozarek RA, Sanowski RA. Carcinoma of the esophagus associated with Fanconi's anemia. J Clin Gastroenterol. 1981;3:171-174.
128. Vaitiekaitis AS, Grau WH. Squamous cell carcinoma of the mandible in Fanconi anemia: report of case. J Oral Surg. 1980;38:372-373.
129. Schofield IDF, Worth AT. Malignant mucosal change in Fanconi's anemia. J Oral Surg. 1980;38:619-622.
130. Kennedy AW, Hart WR. Multiple squamous-cell carcinomas in Fanconi's anemia. Cancer. 1982;50:811-814.
131. Helmerhorst FM, Heaton DC, Crossen PE, von Dem Borne AEGK, Engelfriet CP, Natarajan AT. Familial thrombocytopenia associated with platelet autoantibodies and chromosome breakage. Hum Genet. 1984;65:252-256.
132. Kaplan MJ, Sabio H, Wanebo HJ, Cantrell RW. Squamous cell carcinoma in the immunosuppressed patient: Fanconi's anemia. Laryngoscope. 1985;95:771-775.
133. Fukuoka K, Nishikawa K, Mizumoto Y, et al. Fanconi's anemia with squamous cell carcinoma - a case report and a review of literature. Jpn J Clin Hematol. 1989;30:1992-1996.
134. Alter BP, Frissora CL, Halperin DS, et al. Fanconi's anemia and pregnancy. Br J Haematol. 1991;77:410-418.
135. Snow DG, Campbell JB, Smallman LA. Fanconi's anaemia and post-cricoid carcinoma. J Laryngol Otol. 1991;105:125-127.
136. Lustig JP, Lugassy G, Neder A, Sigler E. Head and neck carcinoma in Fanconi's anaemia - report of a case and review of the literature. Oral Oncol Eur J Cancer. 1995;31B:68-72.
137. Koo WH, Knight LA, Ang PT. Fanconi's anaemia and recurrent squamous cell carcinoma of the oral cavity: a case report. Ann Acad Med Singapore. 1996;25:289-292.
138. Hirschman RJ, Schulman NR, Abuelo JG, Whang-Peng J. Chromosomal aberrations in two cases of inherited aplastic anemia with unusual clinical features. Ann Intern Med. 1969;71:107-117.
139. Guy JT, Auslander MO. Androgenic steroids and hepatocellular carcinoma. Lancet. 1973;i:148.
140. Reed K, Ravikumar TS, Gifford RRM, Grage TB. The association of Fanconi's anemia and squamous cell carcinoma. Cancer. 1983;52:926-928.
141. Kozhevnikov BA, Khododorenko CA. Cancer of the mucous membrane of the left side of the mouth associated with congenital hypoplastic Fanconi's anemia in a 14-year-old boy. Vestn Khir. 1986;136:105-106.
142. Doerr TD, Shibuya TY, Marks SC. Squamous cell carcinoma of the supraglottic larynx in a patient with Fanconi's anemia. Otolaryngol Head Neck Surg. 1998;118:523-525.
143. Marcou Y, D'Andrea A, Jeggo PA, Plowman PN. Normal cellular radiosensitivity in an adult Fanconi anaemia patient with marked clinical radiosensitivity. Radiother Oncol. 2001;60:75-79.
144. Ferro MT, Vazquez-Mazariego Y, Ramiro S, et al. Triplication of 1q in Fanconi anemia. Cancer Genet Cytogenet. 2001;127:38-41.
145. Esparza A, Thompson WR. Familial hypoplastic anemia with multiple congenital anomalies (Fanconi's syndrome) - report of three cases. R I Med J. 1966;49:103-110.
146. Aho S. Clinical conferences. Case of Fanconi's anemia. Kyobu Geka. 1980;33:397-399.
147. Romero MG, Ortiz HC. Anemia de Fanconi. Respuesta a dosis bajas de anabolicos y asociation con carcinoma de esofago [Fanconi's anemia. Response to low doses of anabolics and association with carcinomas of the esophagusl. Rev Invest Clin. 1984;36:353-356.
148. Rockelein G, Ulmer R, Kniewald A, Wagner H. Osophaguskarzinom bei Fanconi-syndrom [Esophageal cancer in Fanconi syndrome] Pathologe. 1986;7:343-347.
149. Linares M, Pastor E, Gomez A, Grau E. Hepatocellular carcinoma and squamous cell carcinoma in a patient with Fanconi's anemia. Ann Hematol. 1991;63:54-55.
150. Soravia C, Spilipoulos A. Carcinome épidermoïde de l'oesophage et anémie de Fanconi. Schweiz Med Wochenschr. 1994;124:725-728.
151. Goluchova M, Urban O, Chalupa J. Spinocellular carcinoma in a patient with Fanconi's anemia. Vnitr Lek. 1998;44:280-281.
152. Gendal ES, Mendelson DS, Janus CL, Schlossberg I, Vogel JM. Squamous cell carcinoma of the esophagus in Fanconi's anemia. Dysphagia. 1988;2:178-179.
153. Sicular A, Fleshner PR, Cohen LB, Hirschhorn K, Matra RJ. Fanconi's anemia and esophageal carcinoma. Gullet. 1993;3:60-63.
154. Swift MR, Hirschhorn K. Fanconi's anemia. Inherited susceptibility to chromosome breakage in various tissues. Ann Intern Med. 1966;65:496-503.
155. Hersey P, Edwards A, Lewis R, Kemp A, McInnes J. Deficient natural killer cell activity in a patient with Fanconi's anaemia and squamous cell carcinoma. Association with defect in interferon release. Clin Exp Immunol. 1982;48:205-212.
156. Arnold WJ, King CR, Magrina J, Masterson BJ. Squamous cell carcinoma of the vulva and Fanconi anemia. Int J Gynaecol Obstet. 1980;18:395-397.
157. Ortonne JP, Jeune R, Coiffet J, Thivolet J. Squamous cell carcinomas in Fanconi's anemia. Arch Dermatol. 1981;117:443-444.
158. Wilkinson EJ, Morgan LS, Friedrich EG Jr. Association of Fanconi's anemia and squamous-cell carcinoma of the lower female genital tract with condyloma acuminatum. A report of two cases. J Reprod Med. 1984;29:447-453.
159. Lebbé C, Pinquier L, Rybojad M, et al. Fanconi's anaemia associated with multicentric Bowen's disease and decreased NK cytotoxicity. Br J Dermatol. 1993;129:615-618.
160. de Chadarevian J-P, Vekemans M, Bernstein M. Fanconi's anemia, medulloblastoma, Wilms' tumor, horseshoe kidney, and gonadal dysgenesis. Arch Pathol Lab Med. 1985;109:367-369.
161. Alter BP, Tenner MS. Brain tumors in patients with Fanconi's Anemia. Arch Pediatr Adolesc Med. 1994;148:661-663.
162. Ruud E, Wesenberg F. Microcephalus, medulloblastoma and excessive toxicity from chemotherapy: an unusual presentation of Fanconi anaemia. Acta Paediatr. 2001;90:580-583.
163. Sjarif DR, Revesz T, de Koning TJ, Duran M, Beemer FA, Poll-The BT. Isolated glycerol kinase deficiency and Fanconi anemia. Am J Med Genet. 2001;99:159-160.
164. Ariffin H, Ariffin WA, Chan LI, Lin HP. Wilms' tumour and Fanconi anaemia: an unusual association. J Paediatr Child Health. 2000;36:196-198.
165. Dupuis-Girod S, Gluckman E, Souberbielle J-C, Brauner R. Growth hormone deficiency caused by pituitary stalk interruption in Fanconi's anemia. J Pediatr. 2001;138:129-133.
166. Tercanli S, Miny P, Siebert MS, Hosli I, Surbek DV, Holzgreve W. Fanconi anemia associated with increased nuchal translucency detected by first-trimester ultrasound. Ultrasound Obstet Gynecol. 2001;17:160-162.
167. Puligandla B, Stass SA, Schumacher HR, Keneklis TP, Bollum FJ. Terminal deoxynucleotidyl transferase in Fanconi's anaemia. Lancet. 1978;ii:1263.
168. Dosik H, Steier W, Lubiniecki A. Inherited aplastic anaemia with increased endoreduplications: a new syndrome or Fanconi's anaemia variant? Br J Haematol. 1979;41:77-82.
169. Jacobs P, Karabus C. Fanconi's anemia. A family study with 20-year follow-up including associated breast pathology. Cancer. 1984;54:1850-1853.
170. Zatterale A, Calzone R, Renda S, et al. Identification and treatment of late onset Fanconi's anemia. Haematologica. 1995;80:535-538.
171. van Niekerk CH, Jordaan C, Badenhorst PN. Pancytopenia secondary to primary malignant lymphoma of bone marrow as the first hematologic manifestation of the Estren-Dameshek variant of Fanconi's anemia. Am J Pediatr Hematol Oncol. 1987;9:344-349.
172. Goldsby RE, Perkins SL, Virshup DM, Brothman AR, Bruggets CS. Lymphoblastic lymphoma and excessive toxicity from chemotherapy: an unusual presentation for Fanconi anemia. J Pediatr Hematol Oncol. 1999;21:240-243.
173. Hill LS, Dennis PM, Fairham SA. Adenocarcinoma of the stomach and Fanconi's anaemia. Postgrad Med J. 1981;57:404.
174. Puig S, Ferrando J, Cervantes F, et al. Fanconi's anemia with cutaneous amyloidosis. Arch Dermatol. 1993;129:788-789.
175. Levinson S, Vincent KA. Multifocal osteosarcoma in a patient with Fanconi anemia. J Pediatr Hematol Oncol. 1997;19:251-253.
176. Flowers MED, Doney KC, Storb R, et al. Marrow transplantation for Fanconi anemia with or without leukemic transformation: an update of the Seattle experience. Bone Marrow Transplant. 1992;9:167-173.
177. Bradford CR, Hoffman HT, Wolf GT, Carey TE, Baker SR, McClatchey KD. Squamous carcinoma of the head and neck in organ transplant recipients: possible role of oncogenic viruses. Laryngoscope. 1990;100:190-194.
178. Socie G, Henry-Amar M, Cosset JM, Devergie A, Girinsky T, Gluckman E. Increased incidence of solid malignant tumors after bone marrow transplantation for severe aplastic anemia. Blood. 1991;78:277-279.
179. Pierga JY, Socie G, Gluckman E, et al. Secondary solid malignant tumors occurring after bone marrow transplantation for severe aplastic anemia given thoraco-abdominal irradiation. Radiother Oncol. 1994;30:55-58.
180. Murayama S, Manzo RP, Kirkpatrick DV, Robinson AE. Squamous cell carcinoma of the tongue associated with Fanconi's anemia: MR characteristics. Pediatr Radiol. 1990;20:347.
181. Hamre MR, Kirkpatrick DV, Humbert JR. Squamous cell carcinoma of the tongue in a patient with Fanconi anemia post bone marrow transplant. Pediatr Res. 1989;25:151A.
182. Somers GR, Tabrizi SN, Tiedemann K, Chow CW, Garland SM, Venter DJ. Squamous cell carcinoma of the tongue in a child with Fanconi anemia: a case report and review of the literature. Pediatr Pathol Lab Med. 1994;15:597-607.
183. Millen FJ, Rainey MG, Hows JM, Burton PA, Irvine GH, Swirsky D. Oral squamous cell carcinoma after allogeneic bone marrow transplantation for Fanconi anaemia. Br J Haematol. 1997;99:410-414.
184. Jansisyanont P, Pazoki A, Ord RA. Squamous cell carcinoma of the tongue after bone marrow transplantation in a patient with Fanconi's anemia. J Oral Maxillofac Surg. 2000;58:1454-1457.
185. Cheng NC, van de Vrugt HJ, van der Valk MA, et al. Mice with a targeted disruption of the Fanconi anemia homolog Fanca. Hum Mol Genet. 2000;9:1805-1811.
186. Ayas M, Solh H, Mustafa MM, et al. Bone marrow transplantation from matched siblings in patients with Fanconi anemia utilizing low-dose cyclophosphamide, thoracoabdominal radiation and antithymocyte globulin. Bone Marrow Transplant. 2001;27:139-143.
187. Mondovits B, Vermylen C, Brichard B, Cornu G. Bone marrow transplantation in Fanconi's anemia: about seven cases. Arch Pediatr. 2001;8:801-802.
188. Yakoub-Agha I, Damaj G, Garderet L, et al. Severe oesophagitis after allogeneic bone marrow transplantation for Fanconi's anemia. Bone Marrow Transplant. 2000;26:215-218.
189. Mulvihill JJ, Ridolfi RL, Schultz FR, Borzy MS, Haughton PBT. Hepatic adenoma in Fanconi anemia treated with oxymetholone. J Pediatr. 1975;87:122-124.
190. Corberand J, Pris J, Dutau G, Rumeau J-L, Regnier C. Association d'une maladie de Fanconi et d'une tumeur hepatique. Chez une malade soumise a un traitement androgenique au long cours [Association of Fanconi's disease and hepatic tumor in a patient undergoing long-term androgen treatment]. Arch Fr Pediatr. 1975;32:275-283.
191. Resnick MB, Kozakewich HPW, Perez-Atayde AR. Hepatic adenoma in the pediatric age group. Clinicopathological observations and assessment of cell proliferative activity. Am J Surg Pathol. 1995;19:1181-1190.
192. Schmidt E, Deeg HJ, Storb R. Regression of androgen-related hepatic tumors in patients with Fanconi's anemia following marrow transplantation. Transplantation. 1984;37:452-457.
193. Garel L, Kalifa G, Buriot D, Sauvegrain J. Multiple adenomas of the liver and Fanconi's anaemia. Ann Radiol. 1980;24:53-54.
194. Farrell GC. Fanconi's familial hypoplastic anaemia with some unusual features. Med J Aust. 1976;1:116-118.
195. Chandra RS, Kapur SP, Kelleher J, Luban N, Patterson K. Benign hepatocellular tumors in the young. A clinicopathologic spectrum. Arch Pathol Lab Med. 1984;108:168-171.
196. LeBrun DP, Silver MM, Freedman MH, Phillips MJ. Fibrolamellar carcinoma of the liver in a patient with Fanconi anemia. Hum Pathol. 1991;22:396-398.
197. Ortega JJ, Olive T, Sanchez C, Giralt J, Serret E. Bone marrow transplant in Fanconi's anemia. Results in five patients. Sangre. 1990;35:433-440.
198. Mokrohisky ST, Ambruso DR, Hathaway WE. Fulminant hepatic neoplasia after androgen therapy. N Engl J Med. 1977;296:1411-1412.
199. Cattan D, Kalifat R, Wautier J-L, Meignan S, Vesin P, Piet R. Maladie de Fanconi et cancer du foie [Fanconi's disease and cancer of the liver]. Arch Fr Mal App Dig. 1974;63:41-48.
200. Abbondanzo SL, Manz HJ, Klappenbach RS, Gootenberg JE. Hepatocellular carcinoma in an 11-year-old girl with Fanconi's anemia. Report of a case and review of the literature. Am J Pediatr Hematol Oncol. 1986;8:334-337.
201. Shapiro P, Ikeda RM, Ruebner BH, Connors MH, Halsted CC, Abildgaard CF. Multiple hepatic tumors and peliosis hepatis in Fanconi's anemia treated with androgens. Am J Dis Child. 1977;131:1104-1106.
202. Kew MC, Van Coller B, Prowse CM, et al. Occurrence of primary hepatocellular cancer and peliosis hepatis after treatment with androgenic steroids. S Afr Med J. 1976;50:1233-1237.
203. Moldvay J, Schaff Z, Lapis K. Hepatocellular carcinoma in Fanconi's anemia treated with androgen and corticosteroid. Zentralbl Pathol. 1991;137:167-170.
204. Recant L, Lacy P. Fanconi's anemia and hepatic cirrhosis. Am J Med. 1965;39:464-475.
205. Johnson FL, Feagler JR, Lerner KG, et al. Association of androgenic-anabolic steroid therapy with development of hepatocellular carcinoma. Lancet. 1972;ii:1273-1276.
206. Cap J, Ondrus B, Danihel L. Focal nodular hyperplasia of the liver and hepatocellular carcinoma in children with Fanconi's anemia after long-term treatment with androgens. Bratisl Lek Listy. 1983;79:73-81.
207. Port RB, Petasnick JP, Ranniger K. Angiographic demonstration of hepatoma in association with Fanconi's anemia. AJR Am J Roentgenol. 1971;113:82-83.
208. Bernstein MS, Hunter RL, Yachnin S. Hepatoma and peliosis hepatis developing in a patient with Fanconi's anemia. N Engl J Med. 1971;284:1135-1136.
209. Bagheri SA, Boyer JL. Peliosis hepatis associated with androgenic-anabolic steroid therapy. A severe form of hepatic injury. Ann Intern Med. 1974;81:610-618.
210. Holder LE, Gnarra DJ, Lampkin BC, Nishiyama H, Perkins P. Hepatoma associated with anabolic steroid therapy. AJR Am J Roentgenol. 1975;124:638-642.
211. Sweeney EC, Evans DJ. Hepatic lesions in patients treated with synthetic anabolic steroids. J Clin Pathol. 1976;29:626-633.
212. Evans DIK. Aplastic anaemia in childhood. In: Geary CG. Aplastic anaemia. London: Bailliere Tindall, 1979:161-194.
213. Ries LAG, Eisner MP, Kosary CL, et al. SEER cancer statistics review, 1973-1998. Bethesda, MD: National Cancer Institute, 2001.
214. Alter BP. Radiosensitivity. in Fanconi's anemia patients. Radiother Oncol. 2002;62:345-347.
215. Maynadie M, Verret C, Moskovtchenko P, et al. Epidemiological characteristics of myelodysplastic syndrome in a well-defined French population. Br J Cancer. 1996;74:288-290.
216. Gillison ML, Koch WM, Capone RB, et al. Evidence for a causal association between human papillomavirus and a subset of head and neck cancers. J Natl Cancer Inst. 2000;92:709-720.
217. Herrero R, Hildesheim A, Bratti C, et al. Population-based study of human papillomavirus infection and cervical neoplasia in rural Costa Rica. J Natl Cancer Inst. 2000;92:464-474.
218. Deeg HJ, Socie G, Schoch G, et al. Malignancies after marrow transplantation for aplastic anemia and Fanconi anemia: a joint Seattle and Paris analysis of results in 700 patients. Blood. 1996;87:386-392.
219. Rosenberg PS, Greene MH, Alter BP. Cancer incidence in persons with Fanconi's anemia. Blood First Edition Paper. Prepublished online 5 September 2002; DOI: 10/1180/blood-2002-05-1498.
220. Liu JM, Kim S, Read EJ, et al. Engraftment of hematopoietic progenitor cells transduced with the Fanconi anemia group C gene (FANCC). Hum Gene Ther. 1999;10:2337-2346.
221. Fanconi anemia. Standards for clinical care. Eugene, OR: Fanconi Anemia Research Fund, 1999.